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Frontonasal dysplasia: A case report

  • Lee, Se Il (Department of Plastic and Reconstructive Surgery, Hanil General Hospital) ;
  • Lee, Seung Je (Department of Plastic and Reconstructive Surgery, Hanil General Hospital) ;
  • Joo, Hong Sil (Department of Plastic and Reconstructive Surgery, Hanil General Hospital)
  • Received : 2019.10.08
  • Accepted : 2019.12.09
  • Published : 2019.12.20

Abstract

Frontonasal dysplasia is an uncommon congenital anomaly with diverse clinical phenotypes and highly variable clinical characteristics, including hypertelorism, a broad nasal root, median facial cleft, a missing or underdeveloped nasal tip, and a widow's peak hairline. Frontonasal dysplasia is mostly inherited and caused by the ALX genes (ALX1, ALX3, and ALX4). We report a rare case of a frontonasal dysplasia patient with mild hypertelorism, a broad nasal root, an underdeveloped nasal tip, an accessory nasal tag, and a widow's peak. We used soft tissue re-draping to achieve aesthetic improvements.

Keywords

References

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